The following data is part of a premarket notification filed by Xomed, Inc. with the FDA for Micro-france Liposuction Cannulas.
| Device ID | K992282 |
| 510k Number | K992282 |
| Device Name: | MICRO-FRANCE LIPOSUCTION CANNULAS |
| Classification | System, Suction, Lipoplasty |
| Applicant | XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 -0980 |
| Contact | Martin D Sargent |
| Correspondent | Martin D Sargent XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 -0980 |
| Product Code | MUU |
| CFR Regulation Number | 878.5040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-07 |
| Decision Date | 1999-09-23 |
| Summary: | summary |